Wisconsin Walk & Roll to Cure FSHD

Wisconsin Walk & Roll to Cure FSHD supporting FSHD Society
FSHD Society

About Wisconsin Walk & Roll to Cure FSHD

The 2020 Wisconsin Walk & Roll to Cure FSHD has gone VIRTUAL!


We are going virtual nationwide on September 12, 2020 !

The Wisconsin Chapter of the FSHD Society will be participating in the National Virtual Walk & Roll to Cure FSHD - the only national event focused solely on funding progress for FSH Muscular Dystrophy.

Our world has been highly impacted by the corona virus pandemic, yet our commitment to our families remains the same.

Every step matters. That is why we must continue to look to the future. 

Register to "walk or roll" today, as a virtual team or individual walker. Invite your family, friends, club members, neighbors, co-workers, classmates or congregation to join you. Everyone who registers will be given a free participant page and access to a state-of-the-art fundraising center. From there, you can share your story on social media and via email, and invite others to join you in getting us closer to a cure!

We are working together to make a difference for those living with FSH Muscular Dystrophy!

Date

Starts at:  June 4, 2020 8:00 AM
Ends at:  September 12, 2020 12:00 PM

Location

Your Yard or Neighborhood
Your Favorite Park or Trail
, USA

Contact

Tim Hollenback
WisconsinChapter@FSHDsociety.org

Why Participate?

FSHD affects nearly 1 million men, women and children worldwide, leaving them with the inability to walk, raise their arms, or simply smile. The FSHD Society is the largest network of patients, families, clinicians, researchers and friends - all advocating for FSHD. YOU are the driving force that enables the FSHD Society to support & empower families and to fund groundbreaking research to find treatments and a cure!

How Your Support Makes a Difference

Your support of the FSHD Society will be put to work right away, to push forward the most promising research, help empower patients and families to live stronger, healthier lives, and press the government and major institutions to give FSH muscular dystrophy (FSHD) the funding and attention it deserves. Your support ensures that no patient need ever face this disease alone, and pushes us towards our goal of delivering treatments to our families by the year 2025!

Thank You to our Generous Sponsors!